Corona ionization device and method

ABSTRACT

A corona discharge ionizer device which emits ions generated by corona discharge to a gas flow to be ionized includes a discharge electrode having a pin configured tip portion. A second grid electrode positioned at a spaced distance from the discharge electrode is provided. The grid electrode is preferably formed from a sheet configured material which has at least one hole formed therein adapted and configured to permit the gas flow to pass therethrough. A power supply is coupled to the discharge electrode and grid electrode configured cause ion emission from the discharge electrode. The power supply is preferably an alternating current power supply configured to produce an alternating electric field region in close proximity to the tip portion of the discharge electrode sufficient to cause avalanche breakdown in the gas flowing in close proximity to the tip portion of the discharge electrode.

RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No.61/560,592, filed Nov. 16, 2011 the entire contents of which isexpressly incorporated herein by reference.

GOVERNMENT LICENSE RIGHTS

This invention was made with Government support under HDTRA1-08-C-0010awarded by the Defense Threat Reduction Agency. The Government hascertain rights in the invention.

FIELD OF THE INVENTION

The present invention relates to devices and methods for generatingions. More specifically, the invention relates to devices and methodsfor generating ions using a corona discharge.

BACKGROUND OF THE INVENTION

The ability to ionize gases is useful for a wide range of applicationsincluding many chemical detection applications. Ionization techniques,in which a gas sample is ionized and then separated into constituentparts that can be detected individually, are widely used for gascomposition sensing. Two well-known examples are Ion MobilitySpectrometry (IMS) and Field Asymmetric Ion Mobility Spectrometry(FAIMS), also known as Differential Mobility Spectrometry (DMS). Ionmobility detection techniques tend to be very well suited to measuringtrace constituents of gas mixtures that often consist of a carrier gaswith additional gases mixed in at low concentrations (for examplepart-per-million or part-per-billion levels). Ion mobility techniquescan also be used effectively over a range of gas pressures, includingpressures close to one atmosphere. This makes them useful for, amongstother things, measuring low-level impurities in air. Because they workby measuring properties of ionized molecules and because gas samples foranalysis generally consist mainly of neutral molecules,ion-mobility-based detectors generally incorporate an ionizer. Thesample gas is passed through the ionizer to produce a population ofionized molecules that are then manipulated in some way involvingseparation or selection of ionized molecules according to their behaviorin an electric field, before being detected. Ionizers commonly in useinclude radioactive sources, light-based devices such as ultra-violetlamps, and electrostatic devices such as corona discharge ionizers.

Radioactive sources have long been used as ionizers for chemicaldetection systems. It is noted radioactive isotopes such as ²⁴¹Am or⁶³Ni are commonly used as ionization sources to generate ions in asurrounding gas stream. Advantages of radioactive sources as ionizersinclude stable and well-understood ion chemistry and the ability toionize without an external power source. A major drawback, however, isthat radioactive sources pose a health hazard and are therefore notsuitable for use in many applications and are subject to strictgovernment regulation. Non-radioactive ionizers, including coronadischarge ionizers, do not suffer from this disadvantage and can bewidely and safely deployed in a range of applications.

A commonly used ion source in the field of chemical detection is theradioactive isotope ⁶³Ni. The interactions of ionizing radiation emittedby ⁶³Ni with many types of gas molecules have been studied andunderstood, meaning that the ion species produced when a ⁶³Ni sourceionizes a gas mixture of a given composition can generally be predictedwith high confidence. ⁶³Ni can therefore be thought of as a “reference”ionizer for many gas detection systems. Radioactive ionization sourceshave the advantage of simplicity, compactness, durability, andreliability. The regulations associated with these radioactiveionization sources, however, may render the incorporation of radioactiveisotopes into a product commercially unfeasible. Therefore, there existsa need for an ionizer that has similar ionization properties to ⁶³Ni butthat does not suffer from the safety and regulatory drawbacks associatedwith radioactive sources.

It is also to be appreciated that electric field ionization has theadvantage of a relatively simple design, relatively simple fabrication,and low power consumption. For instance, in electric field ionization, alarge electric field typically between 10⁷ to 10⁸ V/m is generatedbetween two electrodes. The large magnitude of the electric fieldaccelerates any ions or other free charges within the field therebycausing the accelerated ions or other charges to collide withsurrounding gas molecules. The collision of an accelerated ion or othercharged particle (such as an electron) and a gas molecule creates anionized molecule. A corona discharge is a type of electric fieldionization where a neutral fluid such as, for example, air is ionizednear an electrode having a high electric potential gradient. Such apotential gradient is achieved by using a discharge electrode having asmall radius of curvature. The polarity of the discharge electrodedetermines whether the corona is a positive or negative corona.Typically, the corona has a plasma region and a unipolar region. In theplasma region, electrons avalanche to create more electron/ion pairs. Inthe unipolar region, the slowly moving massive (relative to the electronmass) ions move to the passive electrode, which is usually grounded. Ifthe plasma region grows to encompass the passive electrode, a momentaryspark or a continuous arc may occur. The spark or arc may damage theelectrodes, produce contaminant ions, and reduce the lifetime of theionization source. Therefore, there remains a need for devices andmethods providing improved ionization.

SUMMARY OF THE INVENTION

In one aspect, a corona discharge ionizer device which emits ionsgenerated by corona discharge to a gas flow to be ionized is describedin which an aspect of the corona discharge ionizer device includes adischarge electrode having a pin configured tip portion. A second gridelectrode is positioned at a spaced distance from the dischargeelectrode. The second electrode is preferably formed from a sheetconfigured material which has at least one hole formed therein adaptedand configured to permit the gas flow to pass therethrough. A powersupply is coupled to the discharge electrode and the second electrodeconfigured to cause ion emission from the vicinity of the dischargeelectrode. The power supply is preferably an alternating current powersupply configured to produce an alternating electric field region inclose proximity to the tip portion of the discharge electrode sufficientto cause avalanche breakdown in the gas flowing in close proximity tothe tip portion of the discharge electrode. The alternating currentpower supply produces free electrons, negative ions and positive ionssuch that when the discharge electrode is caused to repel positive ions,negatively charged bodies from the gas flow are caused to be directedtowards the pin configured tip portion of the discharge electrode andpositively charged bodies from the gas flow are caused to be directedtowards the second electrode. Conversely, when the discharge electrodeis caused to repel negative ions, positively charged bodies from the gasflow are caused to be directed towards the pin configured tip portion ofthe discharge electrode and negatively charged bodies from the gas floware caused to be directed towards the second electrode.

In further optional aspects, a corona discharge ionizer which emits ionsgenerated by corona discharge to a gas flow to be ionized is describedin which an aspect of the corona discharge ionizer device includes alight source adapted and configured to provide an ultra-violet (UV)output creating seed ions or other free charges in the gas flow.

In a further aspect, a corona discharge ionizer which emits ionsgenerated by corona discharge to a gas flow to be ionized is describedwhich includes a discharge electrode having a pin configured tip portionwherein the discharge electrode has a hollowed body portion. A secondelectrode is positioned at a spaced distance from the dischargeelectrode. A power supply is coupled to the discharge electrode and thesecond electrode configured to cause ion generation from the vicinity ofthe discharge electrode. An ultra-violet (UV) light-emitting element isdisposed in the hollowed body portion of the discharge electrode adaptedand configured to provide a UV light output from the discharge electrodecreating seed ions in the gas flow surrounding the discharge electrode.

In still another aspect, a corona discharge ionizer which emits ionsgenerated by corona discharge to a gas flow to be ionized is describedwhich includes a discharge electrode having a pin configured tip portionand a second electrode positioned at a spaced distance from thedischarge electrode. An AC power supply and a method of creating avariable DC offset are coupled between the discharge electrode and thesecond electrode. The method of creating the DC offset can include acapacitor and/or a power supply between the discharge electrode and/orthe second electrode whereby a mode balancing DC offset voltage isprovided between the discharge electrode and the second electrode.

BRIEF DESCRIPTION OF THE DRAWINGS

The objects and features of the invention can be understood withreference to the following detailed description of an illustrativeembodiment of the present invention taken together in conjunction withthe accompanying drawings in which:

FIG. 1 is an illustrated embodiment of the invention depicting a coronaionizer;

FIG. 2 depicts an exemplary corona drive waveform for the ionizer ofFIG. 1;

FIG. 3 depicts a schematic representation of a chemical spectrometerusing the corona ionizer of FIG. 1;

FIG. 4 depicts a cross section of a corona ionizer in accordance with anillustrated embodiment of the invention having UV assistance providedvia a low-pressure gas discharge bulb;

FIGS. 5-7 depict a corona ionizer having UV assistance using an opticalfiber in an accordance with illustrated embodiments of the invention;

FIG. 8 depicts a corona ionizer as part of a FAIMS chemical detector anda graph illustrating voltages versus time applied to the FAIMS filterand corona ionizer electrode in accordance with the invention for asequence of positive and negative ion mode sweeps;

FIGS. 9A-9C, 10A, 10B, 11 and 12 illustrate various alternativeembodiments of a corona ionizer in accordance with the invention; and

FIG. 13 depicts integration of corona pin and grid alongside a FAIMSchip and detector electrode into an integrated package in accordancewith the present invention.

WRITTEN DESCRIPTION OF CERTAIN EMBODIMENTS OF THE INVENTION

The present invention is now described more fully with reference to theaccompanying drawings, in which an illustrated embodiment of the presentinvention is shown wherein like reference numerals depict like elements.The present invention is not limited in any way to the illustratedembodiment as the illustrated embodiment described below is merelyexemplary of the invention, which can be embodied in various forms, asappreciated by one skilled in the art. Therefore, it is to be understoodthat any structural and functional details disclosed herein are not tobe interpreted as limiting, but merely as a basis for the claims and asa representative for teaching one skilled in the art to variously employthe present invention. Furthermore, the terms and phrases used hereinare not intended to be limiting but rather to provide an understandabledescription of the invention.

Where a range of values is provided, it is understood that eachintervening value, to the tenth of the unit of the lower limit unlessthe context clearly dictates otherwise, between the upper and lowerlimit of that range and any other stated or intervening value in thatstated range is encompassed within the invention. The upper and lowerlimits of these smaller ranges may independently be included in thesmaller ranges is also encompassed within the invention, subject to anyspecifically excluded limit in the stated range. Where the stated rangeincludes one or both of the limits, ranges excluding either both ofthose included limits are also included in the invention.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention belongs. Although any methods andmaterials similar or equivalent to those described herein can also beused in the practice or testing of the present invention, exemplarymethods and materials are now described. All publications mentionedherein are incorporated herein by reference to disclose and describe themethods and/or materials in connection with which the publications arecited.

It must be noted that as used herein and in the appended claims, thesingular forms “a”, “an,” and “the” include plural referents unless thecontext clearly dictates otherwise. Thus, for example, reference to “astimulus” includes a plurality of such stimuli and reference to “thesignal” includes reference to one or more signals and equivalentsthereof known to those skilled in the art, and so forth.

The publications discussed herein are provided solely for theirdisclosure prior to the filing date of the present application. Nothingherein is to be construed as an admission that the present invention isnot entitled to antedate such publication by virtue of prior invention.Further, the dates of publication provided may differ from the actualpublication dates which may need to be independently confirmed.

Starting with reference to FIG. 1, shown is an illustrated embodiment ofthe invention depicting a corona discharge ionizer device 100. Asillustrated, gas 102 flows in into the device 100 at an entry portion104 of the gas tube 106 for the device 100, and flows around a pinelectrode 108. It is to be understood and appreciated that the pinelectrode 108 (e.g., a discharge electrode) has a moderately sharp tip110 preferably configured to have a radius of curvature in the range10-200 microns. Downstream in the gas flow 102 of the pin electrode 108is a grid electrode 112. The grid electrode 112 is preferably formedfrom a metal sheet (but it is not to be understood to be limitedthereto) having one or more holes 114 formed therethrough, eachconfigured and adapted to permit gas 102 to flow therethrough.

It is to be understood and appreciated that the separation between thepin electrode 108 and the grid electrode 112 is a parameter that affectsionization performance for device 100. An exemplary separation betweenthe pin 108 and the grid electrode 112 is 0.5 to 4 mm.

As illustrated in FIG. 1, the pin electrode 108 and grid electrode 112are each preferably electrically coupled to an alternating current powersupply 116 adapted and configured to apply an oscillating voltagebetween the pin electrode 108 and grid electrode 112. In accordance withthe illustrated embodiment of the device 100, the oscillation frequencyof the alternating current power supply 116 is typically in the range 10to 100 kHz and the AC zero-to-peak voltage is typically in the range 1to 5 kV. It is to be understood operation of the aforesaid alternatingcurrent power supply 116 is not to be understood to be limited toaforementioned operating values.

It is to be understood the high voltage AC signal applied between pinelectrode 108 and grid electrode 112, via the alternating current powersupply 116, in combination with the tip 110 of the pin electrode 108,produces a region of high alternating electric field 118 in closeproximity to the tip 110 of the pin electrode 108 (the corona region).Within this region, the electric field reaches values high enough tocause avalanche breakdown in the gas 102, producing separated positiveand negative charges, which in other words is a mixture of freeelectrons, negative ions and positive ions.

With reference now to FIG. 2 (and with continuing reference to FIG. 1),the oscillation period of the alternating current power supply 116 isshown divided into three intervals: a “positive ion interval” 210 duringwhich the pin electrode 108 is at a high positive voltage with respectto grid electrode 112, a “negative ion interval” 212 during which thepin electrode 108 is at a high negative voltage with respect to the gridelectrode 112, and a “non-ionizing interval” 214 during which thevoltage between the pin electrode 108 and grid electrode 112 is suchthat the electric field in region 118 is not high enough to produceionization of the gas flow 102.

It is to be appreciated that during the positive ion interval 210 thereis a strong electric field in the region 118 in close proximity to thetip 110 of the pin electrode 108, leading to avalanche breakdown of thenearby gas flow 102 causing generation of positive ions, free electronsand negative ions. It is noted the strong electric field drivesnegatively charged bodies very rapidly towards the conductive tip 110 ofthe pin electrode 108, where their excess charge is carried away via theconductor of the pin electrode 108. Conversely, positively chargedbodies are thus driven rapidly away from the tip 110 of the pinelectrode 108 towards the region of lower electric field in closerproximity to the grid electrode 112. Hence, during the positive ioninterval 210, both positive and negative free charges (ions andelectrons) are generated, but only positive ions can escape thehigh-field region 118 in close proximity to the tip 110 of the pinelectrode 108.

During the negative ion interval 212 produced via AC power supply 116,the opposite of the positive ion interval 210 occurs. Again, bothpositive and negative free charges are generated from the gas flow 102,but the positive charges (ions) are rapidly driven into the pinelectrode 108, which is now at a high negative voltage with respect tothe grid electrode 112. The negative charges (ions and free electrons)can escape towards the lower-field regions in close proximity to thegrid electrode 112.

And during the non-ionizing interval, the electric field produced via ACpower supply 116 surrounding the pin electrode 108 is not strong enoughto create avalanche breakdown of the gas flow 102, thus no ionizationoccurs. It is noted that existing free charges are, however, still swepteither toward or away from the pin electrode 108 according to theirpolarity and the polarity of the voltage of the pin electrode 108.

It is to be further appreciated the above mentioned transition betweenperiods when positive ions can escape the ionization region and periodswhen negative ions can escape occurs repeatedly and rapidly—typically ata frequency of approximately 30 kHz (the frequency at which the AC powersupply 116 operates). Thus, a result is creation of a cloud of freepositive and negative charges in and around the ionization region 118.

In accordance with the above descriptions of FIGS. 1 and 2, and withreference now to FIG. 3, when the effect of gas flow is superimposedaround the pin electrode 108 and through one or more holes 114 in thegrid electrode 112, this resulting cloud of charges is swept along withthe neutral gas molecules through the grid electrode 112, toward theexit region 119 of the ionizer device 100. It is to be appreciated thatthere are losses in the ion population due to recombination (e.g. anelectron combining with a positive ion to produce a neutral molecule)and charge loss to conducting surfaces such as the grid electrode 112.Nevertheless, the gas flowing 102 through the hole(s) 114 in the gridelectrode 112 is generally a mixture of neutral molecules, positive ionsand negative ions. This mixture 300 can then be used as the input to anion separation stage 302 (such as a FAIMS filter or IMS drift tube)followed by a detection stage 304, to produce a tunable chemicaldetector 306.

It is to be understood and appreciated that gas discharge can beunstable and as a result of this prior art corona systems have utilizeda method of limiting the potential for the corona to arc which candamage and prematurely age the corona electrodes. Typically, thiscontrol was accomplished via closed loop control, a large seriesresistor in the case of DC corona, a dielectric barrier covering oneelectrode (to stop an arc forming) or the use of very high frequency RF(where the time of each cycle is insufficient for an arc to form).

It is to be appreciated the present invention restricts the pinelectrode 108 to grid voltage 112 by configuring the corona geometry tobe stable thus enabling the use of an open loop which does not obstructthe corona current directly. The threshold voltage is periodically foundby using the FAIMS system or other suitable spectrometers or sensors(such as those disclosed in U.S. Patent Application Nos.: 2011/056371and 2008/017791, each of which is hereby incorporated by reference inits entirety) to detect the threshold (as measuring the AC coronacurrent is difficult in a low-cost and low-power device). It is notedthat the pin electrode 108 to grid electrode 112 geometry provides asignificant electric field gradient (i.e. stable corona region) and thisin turn enables the use of relatively large radius pin electrodes 110which are more geometrically stable in the aggressive coronaenvironment. A larger radius pin electrode provides a larger ionizationvolume, which is beneficial for coupling ions out of the ionizer.Additionally, a larger radius pin electrode provides a more uniformelectric field thereby avoiding very high peak fields, which can lead toundesirable byproduct formation.

Continuous Positive and Negative Ion Generation

As explained above, the instantaneous ion flow from a corona dischargeionizer consists of ions of one sign—either positive or negativedepending on the polarity of the pin electrode. Because ions aregenerated very close to the pin electrode and because the electric fieldin the vicinity of the pin electrode is very strong and becomes strongeras the surface of the pin electrode is approached, ions that have theopposite polarity to the pin electrode will not escape the ionizationregion with their charge intact. Thus, a DC corona discharge ionizerwill produce useful ions of only one polarity at a given time.

In ion-based chemical detection systems, useful information is generallycontained in the signatures of both positive and negative ions in thegas mixture. Therefore it is useful to have an ion source that cangenerate ions of both signs. This is the case for both radioactive ionsources and UV ion sources, as neither relies on a strong electrostaticfield for ion generation.

In accordance with an illustrated embodiment of the present invention,the corona discharge source uses a high-frequency alternating electricfield for ion generation, generating rapid alternating cycle of usefulpositive and negative ion generation. At typical data samplingfrequencies for chemical spectrometers, the effects of these rapidalternations are averaged out whereby the AC corona source behavesessentially as a continuous source of both positive and negative ions.Therefore a single corona ion-source and power supply providesgeneration of chemical spectra in both positive and negative ion modes.It also eases detection system design constraints as the AC coronasource can, in this respect, serve as a drop-in replacement for othercontinuous ion sources such as radioactive or UV-based ionizers.

It is mentioned some prior art corona-based ionizers use a pulsedconfiguration, in which ions are generated in short bursts, as thecorona drive signal is pulsed. The AC corona source in accordance withthe present invention has an advantage over these arrangements as itallows essentially continuous ion generation. It is to be appreciated acontinuous stream of ions is useful for the operation oftunable-filter-type chemical spectrometers such as those based on FAIMS.Further, continuous generation of positive and negative ions is alsoadvantageous in ion based analytical systems because the simultaneouspresence of both polarities can reduce or eliminate the accumulation ofcharges on surfaces along the flow path. Charge accumulation on flowpath surfaces is generally an undesirable effect that adversely affectsperformance. The presence of both ion polarities tends to dischargeaccumulations of charge that would otherwise form, especially when thepolarities are in more balanced proportions.

Transfer of Reactant to Product Ions for Both Positive and Negative Ions

Ion mobility detection techniques often rely on a process known asAtmospheric Pressure Chemical Ionization (APCI) to produce the ionpopulation for analysis. In this process, the ion source producesprimary ions, known as reactant ions, from the carrier gas (often air).These ions interact with the gas mixture through collisions and chargetransfer to produce secondary ions known as product ions. It is oftenthe product ions that are useful in chemical detection. In applicationsinvolving the detection of low-level contaminants in a carrier gas, theprobability of direct ionization of the contaminant molecules is oftenvery low. However, the process of APCI can result in the transfer ofsignificant amounts of charge to the contaminant molecules, givingenough product ions to form a detectable signal. This process relies onthe reactant ions being able to give up their charge to contaminantmolecules by collisional interactions. However, positive reactant ionsshould have relatively low proton affinities and negative reactant ionsshould have relatively low electron affinities. It is noted manycorona-based ionizers are not capable of generating sufficient numbersof negative ions with low-enough electron affinities to give up theircharge to contaminants in the carrier gas. For applications involvingdetection of impurities in air, existing corona-based systems will oftenrespond in the negative ion mode only to the air itself and tobyproducts formed from the air by the corona discharge. Thus, thisstrong response to the carrier gas can mask contaminants that wouldotherwise appear in the negative ion mode. It is noted reactant ionswith very high electron affinities that are often produced in negativecoronas include NO₂ ⁻ and NO₃ ⁻.

For efficient detection of many trace contaminants in the negative ionmode, it is often desirable to generate large quantities of O₂ ⁻ ions.It is to be understood and appreciated that the corona ionizer is ableto generate significant quantities of O₂ ⁻ ions such that the ionizerproduces significant quantities of low-electron-affinity negative-modeions. Therefore, providing the ability to produce strong negative-moderesponses from a continuous corona discharge source is a unique andnovel aspect of the present invention ionizer. For instance, this isadvantageous in that it is particularly useful in the detection ofcertain chemicals including a number of toxic industrial chemicals,explosives and chemical warfare agents.

Control Methodology to Ensure Consistent Ion Chemistry

It is to be understood and appreciated that the mix of output ions fromthe present invention ionizer is a function of corona drive voltage,especially for the negative ions. In brief, using drive voltages closeto the corona threshold voltage (the lowest voltage at which thedischarge is self-sustaining), a significant number of beneficial O₂ ⁻ions are produced. As the drive voltage increases, the proportion of O₂⁻ ions typically rapidly decreases, being replaced by NO₂ ⁻, NO₃ ⁻ andother ion species with high electron affinities. Thus, the presentinvention ionizer performs optimally, especially in the negative mode,when operated close to the corona threshold voltage. It is noted thatthe drive voltage preferably should be adjusted between 10% and 30%above the threshold to ensure stable ion output.

It is further noted that the threshold voltage for corona discharge is afunction not only of electrode geometry, but also of environmentalparameters including pressure and temperature. It is to be appreciatedthe corona threshold voltage is typically proportional to the squareroot of gas pressure and inversely proportional to the square root ofgas temperature. To ensure optimal operation of the ionizer, anillustrated embodiment of the present invention uses a method foradjusting the corona control voltage as follows (and which is not to beunderstood to be the only method for doing so):

-   -   1. Establish the corona threshold voltage (switch-off voltage),        V_(th), at a known temperature T₀ and pressure P₀,    -   2. During operation of the detector periodically measure the        actual temperature T and pressure P in or close to the corona        region; and    -   3. Set the drive voltage of the corona ionizer to a value equal        to A×V_(th)×sqrt(PT₀/P₀T), where A is a pre-determined constant,        generally in the range 1.1 to 1.3.        The above illustrated and exemplary method ensures that the        ionizer is operated in a way that provides a relatively constant        and optimal mix of reactant ions for chemical detection in both        ion modes. The above describes one preferred embodiment and is        not to be understood to be limited thereto.        Fine-Tuning of Corona for in-Service Compensation for Electrode        Ageing and Environmental Effects

It is to be understood that over the lifetime of a corona ionizer, itsthreshold voltage will slowly change due to erosion and oxidation of theelectrodes. Typically, the pin electrode is repeatedly bombarded byhigh-energy charged particles, which cause local heating and ejectionand re-deposition of material from the tip (sputtering). This changesthe shape of the tip of the pin electrode and thus alters the electricfield profile surrounding it. By-products from reactions between thecorona discharge and the carrier gas as well as chemicals deliberatelyor accidentally introduced to the system can cause chemical changes tothe electrodes, such as oxidation. Additionally, effects such ashumidity will affect threshold performance of the pin electrode.

Therefore, these effects combine to produce a shift (generally anincrease) in the threshold voltage of the device over its servicelifetime. In accordance with an illustrated embodiment of the presentinvention, an exemplary method for compensation can be employed when theionizer is switched off, as follows:

-   -   1. Starting from the “on” state of the ionizer, step the drive        voltage down in small decrements while monitoring the ion        current output from the ionizer;    -   2. Record the voltage at which the ionizer switches off during        this ramp-down—i.e. the first voltage at which there is no        measurable ion current output in either ion mode;    -   3. Record the pressure and temperature of the gas in or close to        the ionizing region at the point when switch-off occurred; and    -   4. Use these recorded values as the new values of V_(th), P₀ and        T₀ for the system.        Therefore, employing regular re-calculation of the threshold        voltage, the ion chemistry and output intensity of the source        can be kept more constant over the lifetime of the electrodes.        Alternative Pin Design for Stable Operation

An alternative pin electrode design to that shown in the illustratedembodiment of FIG. 1, which will maintain a more stable radius as itages, is to use the tip of a narrow wire (for example 0.1 mm diameter).After a short ‘burn-in’ period the radius of the end of the wire willremain essentially unchanged as the wire is eroded. If necessary thisfine wire can be mounted on or fabricated as part of a wider diameter‘pin’ for ease of mounting.

Low Duty Cycle Operation for Power Management

It is to be appreciated a key feature of a miniature FAIMS system is afast response time which combined with low duty cycle operation canreduce power consumption without compromising response time. In anillustrated embodiment of the present invention, and when in lowduty-cycle mode, the corona ionizer, gas pump and FAIMS filter drivercircuitry are preferably operated in short bursts—each burst ofoperation preferably being sufficient to take one or more FAIMS spectra.Thus, the present invention ionizer is capable of acquiring a pair ofion sweeps (one positive-mode, one negative-mode) in approximately twoseconds. This fast data acquisition time allows very low duty-cycle (andhence low average power) operation without undue compromises in responsetime. It is noted low-duty-cycle operation relies upon prompt andrepeatable initiation of the corona. Exemplary approaches to facilitatethis are described below.

Simple UV-Assist Arrangement for Consistent, Fast Initiation

It is to be appreciated an ion source for use in a chemical detectionsystem or for other applications should have the ability to switch onand start generating ions within a known, predictable time period. Inmany applications there is a need to use the ionizer conservatively, forexample to conserve system power in a battery-powered chemical detector.In these situations it is typically important that the ionizer shouldswitch on and produce a stable stream of ions preferably in a short timeafter voltage is applied to the electrodes. It is noted to be robustlyable to initiate corona at low field, over a wide range of humiditiesand after long periods of standby, a small amount of seed ions iscreated which results in robust corona initiation.

It is recognized there are many methods of creating UV light with anenergy high enough to liberate electrons from a surface via thephotoelectric effect or to ionize gas molecules directly. Such methodsinclude using UV LEDs and other methods using gas discharge bulbs.However, in accordance with an illustrated embodiment of the presentinvention a capacitively coupled low pressure gas discharge lamp (e.g.Hereaus PKR-106) having a UV-transmissive window is used wherein the gasdischarge lamp is mounted close to the corona region to allow the coronadrive electronics to generate a sufficient electric field in thevicinity of the gas discharge lamp to drive the gas discharge lamp. Thisenables operation of the UV bulb without the additional cost, size andweight of a separate drive circuit.

An example implementation is shown in FIG. 4. The light source (e.g.,bulb) 402 protrudes through the wall 404 of the gas flow pipe 406 sothat its UV output illuminates the gas upstream 408 of the coronaionization region. The gas discharge bulb 402 is placed between ahigh-voltage (pin) electrode 410 and a grounded shield electrode 412.The resultant AC electric field inside the gas discharge bulb 402 causesexcitation of molecules, leading to emission of ultra-violet light. Itis to be appreciated a purpose of the UV bulb 402 is to generate seedions, which are very small in number compared with those generated bythe corona. This is particularly advantageous in that the performance ofthe UV initiation system is robust to the precise position of the coronaUV bulb 402 and the combined corona/UV-bulb drive voltage. For exampleno line of sight is required from the bulb to the electrode surfaces. Itis to be further appreciated that in additional variations of thisillustrated embodiment, UV-created ions are directly detected along withor instead of the corona ions

The illustrated embodiment of FIG. 4 relies on a UV source creating seedions in the system gas flow. It is to be further understood thatalternatively, UV light can be used to stimulate photoemission ofelectrons from a solid surface, such as the corona pin electrode. Theseelectrons, if introduced in to the high-electric field region around thecorona pin, will seed avalanche breakdown and initiate the coronadischarge. A noted advantage of using photoelectric emission is that thedischarge can then be initiated using a lower-energy (longer-wavelength)UV source, such as a UV-light-emitting diode (UV-LED). For instance, anexemplary embodiment using a UV-LED positions the LED so as toilluminate the pin and grid electrode surfaces directly, or through aUV-transmissive optical fiber. It is noted that shining light from a 270nm UV-LED on to these electrodes is extremely effective at promotingfast, repeatable corona initiation.

With reference now to FIGS. 5 and 6, yet other illustrated embodimentsof discharge devices (500, 600) are shown which preferably use a UV-LEDto stimulate photoemission and introduces the UV light using an opticalfiber (502, 602). Such a fiber (502, 602) could either be threaded downthe core of a hollow pin electrode 504 (FIG. 5) or, if coated with apartially transmissive electrically conductive coating 604, could itselfform the pin electrode 606 (FIG. 6).

And with reference now to FIG. 7, still another embodiment of adischarge device 700 is illustrated which uses a shaped UV-reflectivesurface 702, which could also serve as the low-curvature electrode(grid), to direct light back to the sharp electrode 704. It is to beunderstood that by correctly profiling the reflective surface 702, theUV light intensity at the sharp electrode 704 can be increased therebyincreasing the supply of photoelectrons from it. Partial absorption ofthe UV light at the reflector 702 may also liberate photoelectrons toassist in initiating corona discharge.

Voltage Biasing for Ion Mode Selection

Although the corona discharge source described in this invention is wellsuited to spectrometer systems filtering and detecting both polaritiesof ions simultaneously it can also work with sensors analyzing eithersingle ion polarities or alternating between opposing ion polaritiessequentially. With reference to FIG. 8, the basic electrode biasingapproach is illustrated at exemplary voltage levels with positive modebiasing on the right 802 and negative mode on the left 804. It is notedthat the positive 802 and negative 804 mode bias voltages need not beequal and opposite and that they can be set to different values tooptimize the system response. It is to be understood that FIG. 8illustrates one mode of operation with alternating positive and negativemode detection through a single detector. In alternative embodiments itis to be appreciated only a single polarity is detected and yet in otheralternative embodiments, simultaneous positive and negative modedetection is achieved using two single polarity detectors operating inparallel.

Capacitive Coupling of Corona Drive Voltage for Ion Mode Equalization

In the biasing scheme described above with reference to FIG. 8, it isnoted there is no DC voltage bias applied between the pin electrode 806and the grid electrode 808. Described herein below is a method ofapplying a beneficial bias between the pin electrode 806 and the gridelectrode 808. In this illustrated embodiment, it is to be understoodthe ratio of the positive and negative mode ion currents generated bycorona discharge is not necessarily equal as it is contingent upon therelative abundance of the positive and negative mode reactant ion peaksand constituent ion mobilities, which depends upon carrier gas andenvironmental factors such as ambient humidity. A method of improvingthe ion balance between the positive and negative mode RIPs is to add acapacitor in series with the corona pin.

With reference now to FIGS. 9A-9C, FIG. 9A illustrates a pin electrode900 to grid electrode 906 configuration. FIG. 9B illustrates the pinelectrode 900 to grid electrode 906 configuration of FIG. 9Aincorporating a series capacitor 904; and FIG. 9C illustrates the pinelectrode 900 to grid electrode 906 configuration incorporating a seriescapacitor 904 of FIG. 9B in parallel with a bias resistor 908 andvoltage bias source 910.

It is to be understood the currents entering the pin electrode 900 froman AC power supply 902 during the two opposing high field regions of thehigh voltage cycle are equal and opposite in the steady state. Thus, thepin electrode 900 accumulates a DC voltage (superimposed on the ACCorona voltage) that tends to reduce the stronger corona mode andenhances the weaker corona mode. It is to be understood this provides amethod of (partially) equalizing the magnitude of the positive andnegative ion modes, which advantageously simplifies system operationwhile reducing byproducts in the negative ion mode. It is to beappreciated a distinction is made between the “drift bias” that buildsup on the capacitor 904 and the controlled bias applied between the pinelectrode 900 and grid electrode 906. That is, as the capacitor 904effectively handicaps the stronger mode it affects the corona initiationbehavior. For example, in a wet environment (which tends to enhance thepositive ion mode) the pin electrode may drift to a bias value thatenhances the negative mode spectrum. If the next time the ionizer isused is in a dry environment, this bias value may no longer beappropriate to the operating conditions. As illustrated in FIGS. 10A and10B, system memory is simply removed by placing a high value resistor908 across the capacitor 904. This resistor 908 is preferably sized sothat in AC operation the current leaking through the resistor 908 has anegligible effect on the pin electrode 900 potential, however when thecorona is powered down the potential on the pin electrode 900 will decayover a period of approximately a few seconds. For instance, typicalvalues include one (1) nanofarad for the capacitor 904 and one (1)gigaohm for the resistor 908. Other illustrated embodiments are depictedin FIGS. 10A and 10B, wherein FIG. 10A depicts an ionizer having a pinelectrode 900 to grid electrode 906 configuration incorporating a seriescapacitor 904 and discharge resistor 908 coupled to a power supply, andFIG. 10B depicts an ionizer having a pin electrode 900 to grid electrode906 configuration of FIG. 10A having a bias resistor 912 and voltagebias source 910 incorporating the discharge resistor 908.

Optimized Corona Grid Geometry for Controlling Ion Chemistry and IonMode Balance

It is to be appreciated that the present invention corona dischargeionizer in accordance with another illustrated preferred embodimentincludes an electrode grid comprising a single central hole having anapproximate diameter between 0.25 and 2 mm. However, the presentinvention corona discharge ionizer is not to be understood to be limitedto this configuration, as it may encompass other configurations, whetherdescribed herein or not.

It is to be appreciated that the aforesaid single central hole ispreferred because ions on the axis of symmetry see no field towards thegrid electrode which thus enables some ions to escape from the coronaregion even during high voltage operation, when ions would normally beswept into the grid electrode. It is further advantageous in that italso facilitates to channel the gas flow through the active coronaregion at the tip of the pin electrode, thus the corona grid electrodeeffectively acts as a mobility filter by allowing ions therethroughbased on their mobility.

Method of Increasing Charge Equilibration Time

It is to be appreciated that in miniature ionizer systems, as the ionsource is moved closer to the ion filter, the charge transferred to theair flow may not have sufficient time to equilibrate with the analytemolecules present in the sample. In other words, there may not besufficient interaction time for charge to be transferred from theReactant Ion Peak (RIP) to the Product Ion Peaks (PIPs) by AtmosphericPressure Chemical Ionization (ACPI). To obviate this occurrence, and inaccordance with an illustrated embodiment of the present invention, byincreasing the length of time that the charge has to fully equilibratewith the analyte in the air, ion current in the PIPs are improved.

In accordance with an illustrated embodiment of the invention, a methodfor achieving this is to increase the distance between the gridelectrode and the ion filter. In one illustrated method, andparticularly where miniaturization is an important parameter, gas flowis diverted through a larger cross sectional area to slow it down andreduce diffusion losses for a given transit time as shown in theillustrated embodiments of FIGS. 11 and 12. Specifically, FIG. 11depicts baffles 950 in the flow path 952 to extend the transit timebetween ionization source and ion filter region to improve transfer ofcharge from RIP to PIP. And FIG. 12 depicts an alternative embodiment tothe ionizer shown in FIG. 11 whereby it includes a different number ofbaffles 952. It is to be understood and appreciated the number ofbaffles can be increased or decreased to change the flow path length asdesired. It is to be further understood and appreciated the baffles 950may be conducting or non-conducting and, in the case of conducting, maybe biased. A preferred embodiment utilizes metallic baffles preferablyat the same potential as the grid electrode.

Integrating CDI Elements into Chip Package

With reference now to the illustrated embodiment of FIG. 13, to furtherminiaturize a corona-discharge FAIMS system, it is to be understoodelements of the corona ionizer are integrated into a chip package 960(the package that holds the FAIMS filter) which is to be understood tosimplify electrical connection to the corona elements. In theillustrated embodiment of FIG. 13, the corona grid electrode 962 is usedas a lid for the chip package 960 which is particularly advantageous asit provides a degree of protection to the chip assembly duringmanufacture while reducing the part count of the assembly.

It is to be understood and appreciated that in an alternative embodimentto that shown FIG. 13, the corona pin electrode and grid electrode areintegrated into a single component for compactness, ease of assembly,cost reduction and/or ease of replacement. It is to be furtherunderstood and appreciated the integrated pin electrode and gridelectrode assembly can be shaped to enable easy installation andreplacement after excessive erosion or contamination. The lid of thechip package may be a grid holder as opposed to a grid electrode itself.The chip package may incorporate a detector electrode for instance.

Synchronized Corona Supply

It is noted that FAIMS often requires a sensitive ion current detectorand corona ionization can create sources of noise ultimately affectingthe signal to noise ratio and detection performance of the system. Oneapproach to obviate this occurrence is to use a shielding device,however this is often difficult in miniature battery powered systems.

In accordance with an illustrated embodiment of the invention, anotherapproach to suppress noise is to synchronize the corona power supplywith the ion current sampling clock to ensure that ion current sensingis conducted at a consistent point with respect to the corona powersupply output. Another noted advantage of this embodiment is it enablesthe use of lower frequency corona power supplies which consume lesspower for a given output voltage.

The above presents a description of a best mode contemplated forcarrying out the present invention corona discharge ionizer device, andof the manner and process of making and using the illustratedembodiments, in such full, clear, concise, and exact terms as to enableany person skilled in the art to which it pertains to make and use thesedevices and methods. The present invention discharge ionizer device is,however, susceptible to modifications and alternative method steps fromthose discussed above that are fully equivalent. Consequently, thepresent invention discharge ionizer device is not limited to theparticular embodiments disclosed. On the contrary, the present inventiondischarge ionizer device encompasses all modifications and alternativeconstructions and methods coming within the spirit and scope of thepresent invention. Thus, optional embodiments of the present inventiondischarge ionizer device may also be said to broadly consist in theparts, elements and features referred to or indicated herein,individually or collectively, in any or all combinations of two or moreof the parts, elements or features, and wherein specific integers arementioned herein which have known equivalents in the art to which theinvention relates, such known equivalents are deemed to be incorporatedherein as if individually set forth.

Where a claim, if any, is expressed as a means or step for performing aspecified function, it is intended that such claim be construed to coverthe corresponding structure, material, or acts described in thespecification and equivalents thereof, including both structuralequivalents and equivalent structures, material-based equivalents andequivalent materials, and act-based equivalents and equivalent acts.

What is claimed is:
 1. An apparatus, comprising: a corona dischargeionizer adapted to emit ions generated by corona discharge to a gas flowto be ionized, which includes: a discharge electrode having a hollowedbody portion; a second electrode positioned at a spaced distance fromthe discharge electrode; a power supply coupled to the dischargeelectrode and the second electrode, the power supply adapted andconfigured to generate ions in the vicinity of the discharge electrode;and an ultraviolet (UV) light source positioned in proximity to thedischarge electrode such that UV light is directed through the hollowedbody portion whereby the UV light is directed through an optical fiber.2. The apparatus as recited in claim 1, wherein the power supply is analternating current (AC) power supply.
 3. An apparatus as recited inclaim 2, wherein the UV light source is coupled to the AC power supply.4. An apparatus as recited in claim 2, wherein at least one of thedischarge electrode and the second electrode assist in powering the UVsource.
 5. The apparatus as recited in claim 1, wherein the secondelectrode is formed from a sheet configured material which has at leastone hole formed therein adapted and configured to permit gas flow topass therethrough.
 6. The apparatus as recited in claim 1, wherein thedischarge electrode has a pin configured tip portion.
 7. The apparatusas recited in claim 1, wherein the UV light source is a lamp.
 8. Theapparatus as recited in claim 7, wherein the lamp is a gas dischargeultraviolet (UV) lamp.
 9. The corona discharge ionizer as recited inclaim 1, wherein the UV light source is a light emitting diode (LED).10. The apparatus as recited in claim 1, wherein the UV light source isa laser.
 11. The apparatus as recited in claim 1, wherein the UV lightsource is adapted to provide direct illumination.
 12. An apparatus asrecited in claim 1, wherein the optical fiber is provided with apartially UV transmissive conductive coating.
 13. An apparatus asrecited in claim 12, wherein a portion of the conductive coating forms apin configured tip portion of the discharge electrode.
 14. An apparatusas recited in claim 1, wherein the second electrode has a surfaceportion adapted and configured to reflect and concentrate UV light ontothe discharge electrode.
 15. An apparatus as recited in claim 1, whereinthe UV light source is adapted to provide illumination in vicinity of atleast one of the discharge electrode and the second electrode.
 16. Anapparatus as recited in claim 1, wherein the UV light source is adaptedto provide illumination in an area upstream in the gas flow relative tothe discharge electrode and the second electrode.
 17. An apparatus asrecited in claim 1, further including an additional electrode assemblyseparate from the discharge electrode and/or the second electrode, theadditional electrode assembly coupled to an AC power supply and adaptedto assist in powering the UV source.
 18. An apparatus as recited inclaim 1, wherein the UV light source is coupled to a second power supplyseparate from the corona discharge power supply.
 19. An apparatus asrecited in claim 1, further including a tubular structure adapted andconfigured to direct gas flow therethrough.
 20. An apparatus as recitedin claim 1, wherein the UV light source is adapted to provide seed ionsin the gas flow to assist corona discharge.
 21. An apparatus as recitedin claim 20, wherein the UV light source is adapted to generate seedions from the gas flow wherein molecules in the gas flow are ionized byUV light thereby forming at least one of ions and electrons whereby theresulting ions and/or electrons assist with at least one of initiationand sustainment of the corona discharge.
 22. An apparatus as recited inclaim 20, wherein the UV light source is adapted to generate seed ionsvia photo-assisted ionization wherein electrons are liberated by UVlight from a surface having a work function approximately equal to orless than the photon energy of the UV light causing the emission ofelectrons into an ambient gas environment whereby the resultingelectrons and ions assist with at least one of initiation andsustainment of the corona discharge.
 23. An apparatus as recited inclaim 22, which further includes a material with a work-function that islower than the photon energy of the irradiating UV light, adapted andconfigured to be illuminated by the UV light source, which therebyreleases free electrons to assist initiation of ionization.
 24. Anapparatus as recited in claim 23, wherein the low work-function materialforms at least part of at least one of the discharge electrode and thesecond electrode.
 25. An apparatus as recited in claim 1, wherein thereis no solid insulating barrier provided intermediate the dischargeelectrode and the second electrode.
 26. An apparatus as recited in claim1, wherein the corona discharge ionizer is coupled to a spectrometrysystem.
 27. An apparatus as recited in claim 26, wherein thespectrometry system is a Field Asymmetric Ion Mobility Spectrometer(FAIMS).
 28. An apparatus as recited in claim 26, wherein thespectrometry system is an Ion Mobility Spectrometer (IMS).
 29. Anapparatus, comprising: a corona discharge ionizer adapted to emit ionsgenerated by corona discharge to a gas flow to be ionized, whichincludes: a discharge electrode compromising an optical fiber; a secondelectrode positioned at a spaced distance from the discharge electrode;a power supply coupled to the discharge electrode and the secondelectrode, the power supply adapted and configured to generate ions inthe vicinity of the discharge electrode; and an ultraviolet (UV) lightsource positioned in proximity to the discharge electrode wherein the UVlight is transmitted through the optical fiber.
 30. An apparatus asrecited in claim 29, wherein the power supply is an alternating current(AC) power supply.
 31. The apparatus as recited in claim 30, wherein theUV light source is coupled to the AC power supply.
 32. The apparatus asrecited in claim 30, wherein at least one of the discharge electrode andthe second electrode assist in powering the UV source.
 33. An apparatusas recited in claim 29, wherein the second electrode is formed from asheet configured material which has at least one hole formed thereinadapted and configured to permit gas flow to pass therethrough.
 34. Anapparatus as recited in claim 29, wherein the discharge electrode has apin configured tip portion.
 35. An apparatus as recited in claim 29,wherein the UV light source is a lamp.
 36. An apparatus as recited inclaim 35, wherein the lamp is a gas discharge ultraviolet (UV) lamp. 37.A corona discharge ionizer as recited in claim 29, wherein the UV lightsource is a light emitting diode (LED).
 38. An apparatus as recited inclaim 29, wherein the UV light source is a laser.
 39. An apparatus asrecited in claim 29, wherein the UV light source is adapted to providedirect illumination.
 40. An apparatus as recited in claim 29, whereinthe discharge electrode has a hollowed body portion and the UV light isdirected through the hollowed body portion.
 41. An apparatus as recitedin claim 29, wherein the optical fiber is provided with a partially UVtransmissive conductive coating.
 42. An apparatus as recited in claim41, wherein a portion of the conductive coating forms a pin configuredtip portion of the discharge electrode.
 43. The apparatus as recited inclaim 29, wherein the second electrode has a surface portion adapted andconfigured to reflect and concentrate UV light onto the dischargeelectrode.
 44. The apparatus as recited in claim 29, wherein the UVlight source is adapted to provide illumination in vicinity of at leastone of the discharge electrode and the second electrode.
 45. Theapparatus as recited in claim 29, wherein the UV light source is adaptedto provide illumination in an area upstream in the gas flow relative tothe discharge electrode and the second electrode.
 46. The apparatus asrecited in claim 29, further including an additional electrode assemblyseparate from the discharge electrode and/or the second electrode, theadditional electrode assembly coupled to an AC power supply and adaptedto assist in powering the UV source.
 47. The apparatus as recited inclaim 29, wherein the UV light source is coupled to a second powersupply separate from the corona discharge power supply.
 48. Theapparatus as recited in claim 29, further including a tubular structureadapted and configured to direct gas flow therethrough.
 49. Theapparatus as recited in claim 29, wherein the UV light source is adaptedto provide seed ions in the gas flow to assist corona discharge.
 50. Theapparatus as recited in claim 49, wherein the UV light source is adaptedto generate seed ions from the gas flow wherein molecules in the gasflow are ionized by UV light thereby forming at least one of ions andelectrons whereby the resulting ions and/or electrons assist with atleast one of initiation and sustainment of the corona discharge.
 51. Theapparatus as recited in claim 49, wherein the UV light source is adaptedto generate seed ions via photo-assisted ionization wherein electronsare liberated by UV light from a surface having a work functionapproximately equal to or less than the photon energy of the UV lightcausing the emission of electrons into an ambient gas environmentwhereby the resulting electrons and ions assist with at least one ofinitiation and sustainment of the corona discharge.
 52. The apparatus asrecited in claim 51, which further includes a material with awork-function that is lower than the photon energy of the irradiating UVlight, adapted and configured to be illuminated by the UV light source,which thereby releases free electrons to assist initiation ofionization.
 53. The apparatus as recited in claim 52, wherein the lowwork-function material forms at least part of at least one of thedischarge electrode and the second electrode.
 54. The apparatus asrecited in claim 29, wherein there is no solid insulating barrierprovided intermediate the discharge electrode and the second electrode.55. The apparatus as recited in claim 29, wherein the corona dischargeionizer is coupled to a spectrometry system.
 56. The apparatus asrecited in claim 55, wherein the spectrometry system is a FieldAsymmetric Ion Mobility Spectrometer (FAIMS).
 57. The apparatus asrecited in claim 55, wherein the spectrometry system is an Ion MobilitySpectrometer (IMS).